Реакция #56071

ord-697c42f56e994d0894e9a7f91ba0a0c9

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONis added a solution
  2. 2
    ДругоеThe resulting reaction mixture
  3. 3
    Температураis heated at 80°-100° for about 24 hours
  4. 4
    Температураis cooled
  5. 5
    workup.ADDITIONis added
  6. 6
    ДругоеThe layers are separated
  7. 7
    Экстракцияthe alkaline layer extracted with ether
  8. 8
    Промывкаwashed with water
  9. 9
    Сушкаdried over anhydrous sodium sulfate
  10. 10
    Концентрированиеconcentrated under reduced pressure

Методика

To a solution consisting of 2.77 parts of 9-chloro-5-nonyn-2-one in 8 parts by volume of ethanol is added a solution containing 2.77 parts of sodium cyanide dissolved in 4 parts of water. The resulting reaction mixture is heated at 80°-100° for about 24 hours, then is cooled and diluted with ether, whereupon 20 parts by volume of dilute aqueous sodium hydroxide is added with stirring. The layers are separated and the alkaline layer extracted with ether. The ether extracts are combined, then washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 9-cyano-5-nonyn-2-one. This compound exhibits an infrared absorption maximum at 2250 reciprocal centimeters and nuclear magnetic resonance peaks at δ2.18 and δ2.50.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04223158uspto-grants-1980_09